Plasmon-enhanced Spectroscopy Research Articles

Unraveling the multilayer solid-electrolyte interphase in lithium batteries through depth-sensitive plasmon-enhanced Raman spectroscopy: A theoretical and experimental study

The solid-electrolyte interphase (SEI) plays a crucial role in determining the lithium deposition/dissolution behaviors, thus influencing the reversible operation of Li metal batteries renowned for their ultrahigh specific capacity. Recently, we developed a depth-sensitive plasmon-enhanced Raman spectroscopy (DS-PERS) method enabling the in situ and nondestructive characterization of the nanostructure and chemistry of SEI through synergistic plasmonic structures. However, a lack of comprehensive elucidation of the enhancement mechanisms has impeded a detailed understanding of the depth-resolved signal contributions. In this study, we integrate theoretical computations with experimental methodologies to systematically unravel the working principles of the synergistic plasmonic structures, demonstrating that hot spots can effectively detect Raman signals at key locations across various stages of SEI layer evolution. Following Li deposition, the hot spots transfer from the Cu interfaces to the Li interfaces. With the thickening of the deposited Li, the localized surface plasmon resonance of Cu is gradually shielded, leading to the disappearance of hot spots originated from Li-Li coupling. Subsequently, we propose the utilization of Cu@Li-multilayer shell-isolated nanoparticles to compensate and introduce new hot spots, thereby enhancing the depth sensitivity. Our work provides theoretical insights essential for achieving precise depth-resolved PERS characterization.

Plasmon-enhanced Raman spectroscopy to estimate near-electric-field enhancement

Plasmon-enhanced Raman spectroscopy to estimate near-electric-field enhancement

Precise regulation of surface plasmonic hotspots in an Au split nanoring coupled system

The signal enhancement in plasmon-enhanced spectroscopy is primarily contributed by hotspots generated through the surface plasmon resonance effect. Precise control of hotspot positions within nanostructures is of great significance in surface-enhanced Raman spectroscopy (SERS) and high spatial resolution imaging. However, predicting the positions of hotspots is challenging due to the small nanogaps and complex plasmonic interactions. In this study, we theoretically investigate the localized surface plasmonic properties of split ring nanostructure. The effects of variations in the inner radius, gap distance and thickness of the split ring on the hotspot distribution at the nanogaps are systematically analyzed using a three-dimensional finite element method. The results demonstrate that precise control over the positions and quantities of hotspots can be achieved by choosing the excitation wavelength and the gap size of the split rings. The calculated maximum Raman enhancement obtained at the hotspots can reach nine orders of magnitude. Our findings not only contribute to a deeper understanding of the SERS enhancement mechanism, but also provide theoretical insights for further development of surface-enhanced fluorescence, plasmonic sensors, and super-resolution imaging in the field of interface spectroscopy.

Rapid and Facile Synthesis of Gold Trisoctahedrons for Surface-Enhanced Raman Spectroscopy and Refractive Index Sensing.

Au trisoctahedrons (TOHs) with sharp tips and high-index facets have exceptional properties for diverse applications, such as plasmon-enhanced spectroscopies, catalysis, sensing, and biomedicine. However, the synthesis of Au TOHs remains challenging, and most reported synthetic methods are time-consuming or involve complex steps, hindering the exploration of their potential applications. Herein, we present a facile and fast approach to prepare Au TOHs with high uniformity and good control over the final size and shape, all within less than 10 min of synthesis, for surface-enhanced Raman spectroscopy (SERS) and refractive index sensing. The size of the Au TOHs can be easily tailored over a wide range, from 39 to 268 nm, allowing a tuning of the plasmon resonance at wavelengths from visible to near-infrared regions. The exposed facets of the Au TOHs can also be varied by controlling the growth temperatures. The wide tunability of size and exposed facets of Au TOHs can greatly broaden the range of their applications. We have also encapsulated Au TOHs with zeolite imidazolate framework (ZIF-8), obtaining core-shell hybrid structures. With the ability to tune Au TOH size, we further assessed their SERS performances in function of their size by detecting 2-NaT in solution, exhibiting enhancement factors of the order of 105 with higher values when the LSPR is blue-shifted from the laser excitation wavelength. Au TOHs have been also compared for refractive index sensing applications against Au nanospheres, revealing Au TOHs as better candidates. Overall, this facile and fast method for synthesizing Au TOHs with tunable size and exposed facets simplifies the path toward the exploration of properties and applications of this highly symmetrical and high-index nanostructure.

Construction of nanoparticle-on-mirror nanocavities and their applications in plasmon-enhanced spectroscopy.

Plasmonic nanocavities exhibit exceptional capabilities in visualizing the internal structure of a single molecule at sub-nanometer resolution. Among these, an easily manufacturable nanoparticle-on-mirror (NPoM) nanocavity is a successful and powerful platform for demonstrating various optical phenomena. Exciting advances in surface-enhanced spectroscopy using NPoM nanocavities have been developed and explored, including enhanced Raman, fluorescence, phosphorescence, upconversion, etc. This perspective emphasizes the construction of NPoM nanocavities and their applications in achieving higher enhancement capabilities or spatial resolution in dark-field scattering spectroscopy and plasmon-enhanced spectroscopy. We describe a systematic framework that elucidates how to meet the requirements for studying light-matter interactions through the creation of well-designed NPoM nanocavities. Additionally, it provides an outlook on the challenges, future development directions, and practical applications in the field of plasmon-enhanced spectroscopy.

Plasmon-induced magnetic anapole mode assisted strong field enhancement.

Optical metamaterials, sensing, nonlinear optics, and surface-enhanced spectroscopies have witnessed the remarkable potential of the anapole mode. While dielectric particles with a high refractive index have garnered significant attention in recent years, the exploration of plasmonic anapole modes with intense localized electric field enhancements in the visible frequency range remains limited. In this study, we present a theoretical investigation on the relationship between the strongest near-field response and magnetic anapole modes, along with their substantial enhancement of Raman signals from probing molecules. These captivating findings arise from the design of a practical metallic oblate spheroid-film plasmonic system that generates magnetic anapole resonances at frequencies within the visible-near-infrared range. This research not only sheds light on the underlying mechanisms in a wide range of plasmon-enhanced spectroscopies but also paves the way for innovative nano-device designs.

Plasmon-enhanced photoluminescence spectroscopy of a single molecule in the subnanometer cavity

We investigate the influence of quantum tunneling on the plasmon-enhanced electric field and photoluminescence spectroscopy in the subnanometer nanogap between two adjacent Ag nanoparticles using the quantum-corrected method. We analyze the contribution of nonlocal dielectric response at different separation distances to plasmon-enhanced fluorescence using the D-parameters method. Our results demonstrate the high sensitivity of the quantum-induced effect and nonlocal dielectric response to the separation distance. In cases of shorter separation distances, the localized fields start to decrease due to tunneling current short circuit, resulting in a substantial reduction in Raman enhancement. Additionally, the lower quantum yield caused by loss of electron-hole pairs further quenches the fluorescence intensity in the narrowing gaps. We achieve calculated Raman and fluorescence enhancement factors of 13 and 6 orders of magnitude. Under excitation wavelengths of 660 nm, we achieve spatial resolutions of 1.5 nm and 2.2 nm for Raman and fluorescence spectroscopy.

Plasmon-enhanced circular dichroism spectroscopy of chiral drug solutions.

We investigate the potential of surface plasmon polaritons at noble metal interfaces for surface-enhanced chiroptical sensing of dilute chiral drug solutions with nl volume. The high quality factor of surface plasmon resonances in both Otto and Kretschmann configurations enables the enhancement of circular dichroism differenatial absorption thanks to the large near-field intensity of such plasmonic excitations. Furthermore, the subwavelength confinement of surface plasmon polaritons is key to attain chiroptical sensitivity to small amounts of drug volumes placed around ≃100 nm by the metal surface. Our calculations focus on reparixin, a pharmaceutical molecule currently used in clinical studies for patients with community-acquired pneumonia, including COVID-19 and acute respiratory distress syndrome. Considering realistic dilute solutions of reparixin dissolved in water with concentration ≤5 mg/ml and nl volume, we find a circular-dichroism differential absorption enhancement factor of the order ≃20 and chirality-induced polarization distortion upon surface plasmon polariton excitation. Our results are relevant for the development of innovative chiroptical sensors capable of measuring the enantiomeric imbalance of chiral drug solutions with nl volume.

Enhancement and quenching of plasmon-enhanced spectroscopy of single molecule confined in metallic nanoparticle dimers

We present a theoretical analysis of plasmon-enhanced fluorescence (PEF) and Raman scattering (PERS) spectroscopy of a single molecule confined in the laser-irradiated metallic nanoparticles (NPs) dimer, focusing on the origin of the spectral enhancement and quenching effects. The theoretical method of D-parameters has been used to calculate the dimer distance-dependent nonlocal dielectric effect in Ag and Au NPs. Meanwhile, other damping rates and electric field enhancements are quantitatively computed by finite element method. Moreover, PEF and PERS spectra of rhodamine 6G are obtained within the density-functional theory. Our calculated results show that the PERS mainly depend on the excitation and emission field enhancements, and thus it occurs at the narrower dimer gap due to the stronger localized plasmon coupling. The PEF is related to fluorescence rate caused by the competition between excitation electric field and quantum efficiency, and the increase of former may enhance the fluorescence intensity while the lower latter lead to reduce the intensity as decreasing the dimer distance. The contribution of nonlocal dielectric effect can significantly reduce the quantum efficiency at smaller distance so that it overcomes the excitation field enhancement, leading to the fluorescence quenching for Au NPs dimer. Furthermore, by optimizing the dimer distance and NPs size, the maximum PERS and PEF cross sections reach 10−14 and 10−15 under 2.45 eV laser excitation for Ag NPs dimer, and 10−18 for Au NPs. Our study finely explains the experiment results showed either fluorescence enhancement or quenching with the change of molecule-NPs distance, and better guidance for optimizing the experiments.

(Invited) Multiscale Interfacial Heterogeneity Explored by Advanced Spectroscopy and Imaging for Batteries Beyond Lithium-Ion

Keywords: solid-liquid interface, solid-state battery, surface-enhanced Raman spectroscopy (SERS), tip-enhanced Raman spectroscopy (TERS), neutron tomography, sulfide solid-state electrolyte, Raman imagingThe ever-growing needs for energy storage systems require batteries with even higher power and energy density with extended life and enhanced safety beyond the current Li-ion battery technologies. Fulfilling these needs requires new battery chemistries, including high-energy-density electrode materials, solid-state electrolytes, and efficient interphases to mitigate the side reactions between the electrodes and the electrolytes.Charge transport across the electrode and electrolyte interface is believed to be one of the charge/discharge rate-limiting steps. Although the composition, morphology, and structure of solid-electrolyte interphase (SEI) have been extensively studied, probing its evolution at the nanoscale is challenging to a large extent. Plasmon-enhanced Raman spectroscopy (PERS) is promising to solve this challenge. PERS is the resonant oscillation of conduction electrons at the interface between negative and positive permittivity molecules stimulated by incident light. It includes surface-enhanced Raman spectroscopy (SERS) and tip-enhanced Raman spectroscopy (TERS). In the first part of this talk, I will show that gap-mode SERS is ideal to probe salt solvation structure in the immediate vicinity (< 20 nm) of the electrode/electrolyte interface. SERS lacks the nanoscale resolution in the sample plane. This can be compensated by TERS. TERS analysis on cycled high-energy silicon anodes indicates that the nanometer scale SEI "islands" are unevenly distributed. Even for the same SEI "island", the composition is different from point to point with inter-point distance smaller than 10 nm.All-solid-state lithium metal batteries (SSBs) promise specific energy >500 Wh/kg. A solid-state electrolyte (SSE) plays an irreplaceable role in reaching such an energy-density goal. Sulfide-based SSEs have emerged as a prominent class of soft ionic conductors that have comparable room-temperature ionic conductivity to their liquid electrolyte counterparts. However, when paring with a high voltage cathode, such as lithium nickel manganese cobalt oxide (NMC), the (electro)chemical instability of the sulfide SSE at the electrode/SSE interfaces becomes a major challenge. The interfacial instability can result in >50% initial capacity loss in a Li/sulfide SSE/NMC battery, thereby keeping the sulfide SSEs from commercialization. In the second part of this talk, I will show how we synergistically use neutron computed tomography and in situ Raman imaging, with clustering analysis to track lithium displacement at the interface of a sulfide-based SSB. Acknowledgment This research was conducted at Oak Ridge National Laboratory, managed by UT Battelle, LLC, for the U.S. Department of Energy (DOE) and is supported by Asst. Secretary, Energy Efficiency and Renewable Energy (EERE), Vehicle Technologies Office (VTO) through the Advanced Battery Materials Research (BMR) Program. This research used resources at High Flux Isotope Reactor, a DOE Office of Science User Facilities operated by the Oak Ridge National Laboratory.

Scalable trapping of single nanosized extracellular vesicles using plasmonics

Heterogeneous nanoscale extracellular vesicles (EVs) are of significant interest for disease detection, monitoring, and therapeutics. However, trapping these nano-sized EVs using optical tweezers has been challenging due to their small size. Plasmon-enhanced optical trapping offers a solution. Nevertheless, existing plasmonic tweezers have limited throughput and can take tens of minutes for trapping for low particle concentrations. Here, we present an innovative approach called geometry-induced electrohydrodynamic tweezers (GET) that overcomes these limitations. GET generates multiple electrohydrodynamic potentials, allowing parallel transport and trapping of single EVs within seconds. By integrating nanoscale plasmonic cavities at the center of each GET trap, single EVs can be placed near plasmonic cavities, enabling instant plasmon-enhanced optical trapping upon laser illumination without detrimental heating effects. These non-invasive scalable hybrid nanotweezers open new horizons for high-throughput tether-free plasmon-enhanced single EV trapping and spectroscopy. Other potential areas of impact include nanoplastics characterization, and scalable hybrid integration for quantum photonics.

A Full Quantum Mechanical Approach Assessing the Chemical and Electromagnetic Effect in TERS.

Tip-enhanced Raman spectroscopy (TERS) is a valuable method for surface analysis with nanometer to angstrom-scale resolution; however, the accurate simulation of particular TERS signals remains a computational challenge. We approach this challenge by combining the two main contributors to plasmon-enhanced Raman spectroscopy and to the high resolution in TERS, in particular, the electromagnetic and the chemical effect, into one quantum mechanical simulation. The electromagnetic effect describes the sample's interaction with the strong, highly localized, and inhomogeneous electric fields associated with the plasmonic tip and is typically the thematic focus for most mechanistic studies. On the other hand, the chemical effect covers the different responses to the extremely close-range and highly position-sensitive chemical interaction between the apex tip atom(s) and the sample, and, as we could show in previous works, plays an often underestimated role. Starting from a (time-dependent) density functional theory description of the chemical model system, comprised of a tin(II) phthalocyanine sample molecule and a single silver atom as the tip, we introduce the electromagnetic effect through a series of static point charges that recreate the electric field in the vicinity of the plasmonic Ag nanoparticle. By scanning the tip over the molecule along a 3D grid, we can investigate the system's Raman response on each position for nonresonant and resonant illumination. Simulating both effects on their own already hints at the achievable signal enhancement and resolution, but the combination of both creates even stronger evidence that TERS is capable of resolving submolecular features.

Resolving nanostructure and chemistry of solid-electrolyte interphase on lithium anodes by depth-sensitive plasmon-enhanced Raman spectroscopy

The solid-electrolyte interphase (SEI) plays crucial roles for the reversible operation of lithium metal batteries. However, fundamental understanding of the mechanisms of SEI formation and evolution is still limited. Herein, we develop a depth-sensitive plasmon-enhanced Raman spectroscopy (DS-PERS) method to enable in-situ and nondestructive characterization of the nanostructure and chemistry of SEI, based on synergistic enhancements of localized surface plasmons from nanostructured Cu, shell-isolated Au nanoparticles and Li deposits at different depths. We monitor the sequential formation of SEI in both ether-based and carbonate-based dual-salt electrolytes on a Cu current collector and then on freshly deposited Li, with dramatic chemical reconstruction. The molecular-level insights from the DS-PERS study unravel the profound influences of Li in modifying SEI formation and in turn the roles of SEI in regulating the Li-ion desolvation and the subsequent Li deposition at SEI-coupled interfaces. Last, we develop a cycling protocol that promotes a favorable direct SEI formation route, which significantly enhances the performance of anode-free Li metal batteries.

Plasmonic Au-Cu nanostructures: Synthesis and applications.

Plasmonic Au-Cu nanostructures composed of Au and Cu metals, have demonstrated advantages over their monolithic counterparts, which have recently attracted considerable attention. Au-Cu nanostructures are currently used in various research fields, including catalysis, light harvesting, optoelectronics, and biotechnologies. Herein, recent developments in Au-Cu nanostructures are summarized. The development of three types of Au-Cu nanostructures is reviewed, including alloys, core-shell structures, and Janus structures. Afterwards, we discuss the peculiar plasmonic properties of Au-Cu nanostructures as well as their potential applications. The excellent properties of Au-Cu nanostructures enable applications in catalysis, plasmon-enhanced spectroscopy, photothermal conversion and therapy. Lastly, we present our thoughts on the current status and future prospects of the Au-Cu nanostructures research field. This review is intended to contribute to the development of fabrication strategies and applications relating to Au-Cu nanostructures.

Ion-Mediated Protein Stabilization on Nanoscopic Surfaces.

The emergence of nanoparticles in biomedical applications has made their interactions with proteins inevitable. Nanoparticles conjugated with proteins and peptide-based constructs form an integral part of nanotherapeutics and have recently shown promise in treating a myriad of diseases. The proper functioning of proteins is critical to achieve their biological functions. However, interface issues result in the denaturation of proteins, and the loss of orientation and steric hindrance can adversely affect the function of the conjugate. Furthermore, surface-induced denaturation also triggers protein aggregation, resulting in amyloid-like species. Understanding the mechanistic underpinnings of protein-nanoparticle interactions and controlling their interfacial characteristics are critical and challenging due to the complex nature of the conjugates. In this milieu, we demonstrate that ionic liquids can be suitable candidates for stabilizing protein-nanoparticle interactions by virtue of their excellent protein-preserving properties. We also probe the previously unexplored mechanism of ion-mediated stabilization of the protein molecules on the nanoparticle surface. The protein-nanoparticle conjugates consist of lysozyme and choline-based ionic liquids characterized by optical and electron microscopy techniques combined with surface-sensitive plasmon-enhanced Raman spectroscopy. Furthermore, atomistic molecular dynamics simulations of the conjugates delineate interfacial interactions of the protein molecules and the modulation by the ions, particularly the conformational changes and the dynamic correlation when the protein and specific ionic liquid molecules are adsorbed on the nanoparticle surface. The combined experimental and computational studies showed the synergistic behavior of the ions of the ionic liquids, specifically the orientation and coverage of the anions aided by the cations to control the surface interactions and hence the overall protein stability. These studies pave the way for using ionic liquids, particularly their biocompatible counterparts in nanoparticle-based complexes, as stabilizing agents for biomedical applications.

High-speed nanoscale optical trapping with plasmonic double nanohole aperture.

Optical trapping with plasmonic double nanohole (DNH) apertures has proven to be an efficient method for trapping sub-50 nm particles due to their suppressed plasmonic heating effect and very high electric field enhancement in the gap region of the aperture. However, plasmonic tweezers are generally diffusion-limited, requiring particles to diffuse down to a few tens of nanometres from the high field enhancement regions before they can be trapped. The loading of target particles to the plasmonic hotspots can take several minutes for diluted samples. In this work, rapid particle transport and trapping of a 25 nm polystyrene sphere is demonstrated, leveraging an electrothermoplasmonic flow induced upon application of an AC field in the presence of a laser-induced temperature gradient. Using this approach, we demonstrate the rapid transport of a 25 nm polystyrene particle across a distance of 63 μm and trapping at the DNH under 16 s. This platform shows great potential for applications involving simultaneous trapping and plasmon-enhanced spectroscopies, such as Raman enhancement via the intense electric field enhancement in the DNH gap.

Oblique-Incidence-Excited Localized Hot Spots in Plasmonic Particle-on-Film Nanocavities

Regarding plasmonic nanocavities formed by particle-on-film, the nanogap hot spots play an essential role in wide applications including plasmon-enhanced spectroscopy, ultrasensitive sensing, photovoltaics, and photocatalysis. However, hot spots at the nanogap are symmetrically distributed on both sides of the junction under normal incidence. Herein, under the condition of oblique incidence, properties of plasmonic hot spots in the Au@SiO2 particle-on-film have been investigated theoretically. We find that when the plane wave is incident obliquely, the hot spots in the gap are not only symmetrically distributed on both sides of the contact point but also circularly distributed around the junction at specific excitation wavelengths. With the adjustment of the incidence angle, the maximum surface-enhanced Raman spectroscopy enhancement factor from this circularly distributed hot spot reaches 11.3 orders in magnitude. Moreover, the resonant mode at 785 nm has been readily matched by optimizing the size of the Au core, and the optimal thickness of the silica shell with 1 nm for achieving the maximum electromagnetic (EM) field enhancement was further demonstrated. These findings offer a new strategy for manipulating locations of localized hot spots with strong near-field enhancement in plasmonic nanocavities.

Efficient manipulation of plasmonic modes in single symmetry-breaking Ag nanocube

Efficiently manipulating plasmonic modes by adjusting geometry, spatial arrangement, and the nature of the material has shown great potential in wide applications including ultrasensitive sensing, optical modulation, and surface-enhanced spectroscopy. Symmetry breaking as an effective geometry-controlled method can induce plasmonic hybridization and further tune resonant wavelength, strength, and electromagnetic fields. Herein, through introducing cavity along the cubic lateral edges, we theoretically design symmetry-breaking Ag nanocube that is capable of arbitrarily tuning plasmonic modes based on plasmon hybridization theory. Originated from the hybridization of the nanocube and cavity, bonding and anti-bonding dipole–dipole coupled modes simultaneously exhibit trends of blueshifts and redshifts by decreasing the overlapped domain and by increasing the radius of cavity. Moreover, the hybrid modes can be independently tuned by changing the edge length of the cube and the number and the location of cavity. These findings not only advance the understanding of the mechanism of light-matter interactions in symmetry-breaking Ag nanocube but also provide further guidance for designing efficient nanophotonic platforms in plasmon-enhanced spectroscopy and optical wave manipulations.

Toroidal dipole-modulated dipole-dipole double-resonance in colloidal gold rod-cup nanocrystals for improved SERS and second-harmonic generation.

Colloidal metal nanocrystals (NCs) show great potential in plasmon-enhanced spectroscopy owing to their attractive and structure-depended plasmonic properties. Herein, unique Au rod-cup NCs, where Au nanocups are embedded on the one or two ends of Au nanorods (NRs), are successfully prepared for the first time via a controllable wet-chemistry strategy. The Au rod-cup NCs possess multiple plasmon modes including transverse and longitudinal electric dipole (TED and LED), magnetic dipole (MD), and toroidal dipole (TD) modulated LED resonances, producing large extinction cross-section and huge near-field enhancements for plasmon-enhanced spectroscopy. Particularly, Au rod-cup NCs with two embedded cups show excellent surface-enhanced Raman spectroscopy (SERS) performance than Au NRs (75.6-fold enhancement excited at 633 nm) on detecting crystal violet owing to the strong electromagnetic hotspots synergistically induced by MD, LED, and TED-based plasmon coupling between Au cup and rod. Moreover, the strong TD-modulated dipole-dipole double-resonance and MD modes in Au rod-cup NCs bring a 37.3-fold enhancement of second-harmonic generation intensity compared with bare Au NRs, because they can efficiently harvest photoenergy at fundamental frequency and generate large near-field enhancements at second-harmonic wavelength. These findings provide a strategy for designing optical nanoantennas for plasmon-enhanced applications based on multiple plasmon modes.Electronic Supplementary MaterialSupplementary material (SEM image of Au rod-one-cup NCs; TEM image of Au/PbS hybrids; SEM image of Au rod-two-cup NCs; low-amplification SEM image of Au rod-two-cup NCs; experimental extinction and calculated electric field distributions of Au NR excited at different wavelengths; calculated absorption and scattering spectra of Au rod-one-cup NCs; schematic illustration of the cut plane and the corresponding magnetic field distribution under L3 excitation; Raman spectra of CV (10−6 M) adsorbed on Au rod-cup NCs with different cup sizes; calculated magnetic field distribution of Au rodcup NCs excited at 532 and 633 nm; calculated electric field distributions of Au rod-one-cup NC excited at 600 nm along TE and LE; the models of Au rod-cup NCs used in the simulations) is available in the online version of this article at 10.1007/s12274-022-4562-5.

Hybrid composite based on conducting polymers and plasmonic nanomaterials applied to catalysis and sensing

Combining plasmonic and semiconductors offers significant potential in creating sensing and photocatalytic devices. Nanocomposites including both metals and semiconductors can control the charge states in the metals that can enhance catalysis activity along with plasmon-enhanced spectroscopy. Here we demonstrate the use of conducting polymer materials with plasmonic nanomaterials to boost up to five-fold plasmon-enhanced Raman scattering spectroscopy signal strength and support oxidation of target molecules through supporting charge transfer processes. This work demonstrates the use of conducting polymers as a semiconductor platform to support plasmonic catalysis and sensing.